Osteopontin is a Prognostic Factor in Patients with Advanced Gastric Cancer
- PMID: 32881660
- DOI: 10.2174/1386207323666200902135349
Osteopontin is a Prognostic Factor in Patients with Advanced Gastric Cancer
Abstract
Objective: Osteopontin (OPN), a phosphorylated sialoprotein, has been shown to overexpress in a variety of cancers and to contribute tumor progression and metastasis by increasing cell migration and adhesion. In the current study, we aimed to investigate the prognostic and predictive role of OPN in patients with advanced gastric cancer.
Methods: A total of 42 consecutive chemonaive patients with advanced gastric cancer and 29 healthy controls were included. The patients were treated with a modified DCF regimen. The blood samples were obtained before each chemotherapy cycle from the patients and once from the healthy controls. The plasma OPN is measured by ELISA.
Results: The overall response and disease stabilization rates were 25% and 72%, respectively. The median serum OPN level of the patient group was significantly higher compared to healthy controls (176.9 ng/ml (range: 41.5 -521.4) vs 64.3 ng/ml (range 42.1-105.3 ng/ml), p<0.0001). The median overall survival time was 7.0 ± 1.1 (95% CI: 4.9-9.2) months and 1-year overall survival rate was 20.8%. The patients who responded to mDCF had lower plasma OPN levels than the non-responding ones (110.7±29.3 ng/mL, 211.9±24.4 ng/mL respectively, p=0.002). The performance status and the plasma OPN levels were found to be significant factors for overall survival in the multivariate analysis (p=0.004 and 0.016, respectively).
Conclusion: The serum OPN seems to be a novel significant prognostic and predictive factor in patients with advanced gastric cancer who were treated with DCF regimen.
Keywords: Gastric cancer; Osteopontin; biomarker; oncologist; predictive factor; prognostic factor.
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.
Similar articles
-
Elevated plasma osteopontin associated with gastric cancer development, invasion and survival.Gut. 2007 Jun;56(6):782-9. doi: 10.1136/gut.2006.109868. Epub 2006 Dec 5. Gut. 2007. PMID: 17148500 Free PMC article.
-
Osteopontin level and promoter polymorphism in patients with metastatic breast cancer.Curr Oncol. 2020 Oct;27(5):e444-e450. doi: 10.3747/co.27.6449. Epub 2020 Oct 1. Curr Oncol. 2020. PMID: 33173383 Free PMC article.
-
Osteopontin and thrombospondin-1 play opposite roles in promoting tumor aggressiveness of primary resected non-small cell lung cancer.BMC Cancer. 2016 Jul 15;16:483. doi: 10.1186/s12885-016-2541-5. BMC Cancer. 2016. PMID: 27422280 Free PMC article.
-
Osteopontin as potential biomarker and therapeutic target in gastric and liver cancers.World J Gastroenterol. 2012 Aug 14;18(30):3923-30. doi: 10.3748/wjg.v18.i30.3923. World J Gastroenterol. 2012. PMID: 22912540 Free PMC article. Review.
-
Osteopontin: its potential role in cancer of children and young adults.Biomark Med. 2017 Apr;11(4):389-402. doi: 10.2217/bmm-2016-0308. Epub 2017 Mar 14. Biomark Med. 2017. PMID: 28326824 Review.
Cited by
-
Distinctive Prognostic Value and Cellular Functions of Osteopontin Splice Variants in Human Gastric Cancer.Cells. 2021 Jul 19;10(7):1820. doi: 10.3390/cells10071820. Cells. 2021. PMID: 34359989 Free PMC article.
-
Osteopontin promotes gastric cancer progression via phosphatidylinositol-3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway.World J Gastrointest Oncol. 2023 Sep 15;15(9):1544-1555. doi: 10.4251/wjgo.v15.i9.1544. World J Gastrointest Oncol. 2023. PMID: 37746644 Free PMC article.
-
Osteopontin and Cancer: Insights into Its Role in Drug Resistance.Biomedicines. 2023 Jan 12;11(1):197. doi: 10.3390/biomedicines11010197. Biomedicines. 2023. PMID: 36672705 Free PMC article. Review.
-
Aptamers for Proteins Associated with Rheumatic Diseases: Progress, Challenges, and Prospects of Diagnostic and Therapeutic Applications.Biomedicines. 2020 Nov 22;8(11):527. doi: 10.3390/biomedicines8110527. Biomedicines. 2020. PMID: 33266394 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials